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Results:
1-7
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Results: 7
Authors:
WITTINE LM
JOSEPHSON KD
WILLIAMS MS
Citation: Lm. Wittine et al., AORTIC ROOT DILATION IN LUJAN-FRYNS SYNDROME, Journal of investigative medicine, 46(1), 1998, pp. 66-66
Authors:
WILLIAMS MS
JOSEPHSON KD
Citation: Ms. Williams et Kd. Josephson, AN UNUSUAL COMPLICATION OF THE ROTHMUND-THOMSON-SYNDROME, Journal of investigative medicine, 46(1), 1998, pp. 120-120
Authors:
WILLIAMS MS
JOSEPHSON KD
Citation: Ms. Williams et Kd. Josephson, UNUSUAL AUTOSOMAL RECESSIVE LYMPHATIC ANOMALIES IN 2 UNRELATED AMISH FAMILIES, American journal of medical genetics, 73(3), 1997, pp. 286-289
Authors:
ASWEGAN AL
JOSEPHSON KD
MOWBRAY R
PAULI RM
SPRITZ RA
WILLIAMS MS
Citation: Al. Aswegan et al., AUTOSOMAL-DOMINANT HYPOHIDROTIC ECTODERMAL DYSPLASIA IN A LARGE FAMILY, American journal of medical genetics, 72(4), 1997, pp. 462-467
Authors:
PAULI RM
WILLIAMS MS
JOSEPHSON KD
TINT GS
Citation: Rm. Pauli et al., SMITH-LEMLI-OPITZ-SYNDROME - 30-YEAR FOLLOW-UP OF S OF RSH SYNDROME, American journal of medical genetics, 68(3), 1997, pp. 260-262
Authors:
ROBIN NH
FELDMAN GJ
ARONSON AL
MITCHELL HF
WEKSBERG R
LEONARD CO
BURTON BK
JOSEPHSON KD
LAXOVA R
ALECK KA
ALLANSON JE
GUIONALMEIDA ML
MARTIN RA
LEICHTMAN LG
PRICE RA
OPITZ JM
MUENKE M
Citation: Nh. Robin et al., OPITZ-SYNDROME IS GENETICALLY HETEROGENEOUS, WITH ONE LOCUS ON XP22, AND A 2ND LOCUS ON 22Q11.2, Nature genetics, 11(4), 1995, pp. 459-461
Authors:
WILLIAMS MS
JOSEPHSON KD
WARGOWSKI DS
Citation: Ms. Williams et al., 10P TERMINAL DELETION - A PATIENT WITH THE SMALLEST DESCRIBED DELETION AND A REVIEW OF THE LITERATURE, American journal of human genetics, 57(4), 1995, pp. 732-732
Risultati:
1-7
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